FDAnews New Management Report: Implementing an 11-Step Plan for Device Software Validation and Verif
The FDA is cracking down on companies that don't carry out device software verification and validation, issuing an increasing number of 483s and warning letters to manufacturers of medical devices with embedded software, and manufacturers of software used as a device itself. With this new report, readers will find out exactly what FDA inspectors are being trained to look for in terms of device software verification and validation. Falls Church, VA (PRWEB) May 15, 2014 Implementing an 11-Step Plan for Device Software Validation and Verification **FDAnews Management Report** http://ww
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